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Pharmacist graduated at the University of Barcelona and with a Master's degree in Clinical Trial Monitoring. Currently CRA trainee at Pivotal at the Clinical Operations department. With positive and enthusiasthic attitude, efficient in teamworking and good organisational skills. Fluent in Spanish and Catalan (native languages) and advanced English, and basic accredited knowledge of German. Fully willing to learn and to develop my skills and knowledge in the clinical research field. Available for travel and working abroad.


Current Experience

  • CRA Trainee
    Since May 2015
    Receiving training from Clinical operations and Data Management departments. Performing Start-up, Clinical Administrative, Co-monitoring and Data Management tasks.

Past Experience

  • Pharmacist
    December 2013 --- February 2015
    Dispensing drugs and Health care products. Maintaining and improving people's health by providing advice and information as well as supplying prescription medicines, and ensuring that different treatments are compatible. Actively collaborated in health promotion programs. Monitoring blood pressure, cholesterol and glucose levels. Preparation of pharmaceutical compounding. And keeping up to date with current pharmacy practice, new drugs and their uses.

  • Student Research Project
    September 2011 --- July 2012
    Collaboration in a PhD Research Project in the Microbiology department (Faculty of Pharmacy)

  • Research Assistant
    September 2010 --- January 2011
    Research assistant in the Physiology department (FIDAN Group) of the Pharmacy Facutly. Support to PhD students.


Self Assessment :
AssertivenessAttention to detailEfficiencyApproachabilityInterest in knowledgeSelf-disciplineProactivity


Self Assessment :
Clinical operationsClinical trialsEnglishGermanPharmacyGood Clinical Practice (GCP)Microsoft Office Animal modelsClinical study reportsICH GCP guidelinesMicrobiologyspanish
LinkedIn Assessment :
Pharmaceutical IndustryPharmacyMicrosoft OfficeClinical monitoringClinical trialsClinical researchEnglishNormas ICH de buenas pr

Skills and Expertise

Self Assessment :
Monitor a clinical studyArchive documentation Report dataAdministrative supportMonitor clinical trials Manage clinical trial files/documents Build and manage the Trial Master File (TMF)Interpret dataConfirm protocol complianceEnsure good clinical practice (GCP)Verify data


  • Master's degree in Clinical Trial Monitoring from ESAME Pharmaceutical Bussiness School - Universitat de Barcelona in 2015
  • Bachelor of Pharmacy (B.Pharm.) in EHEA bachelor's degree in Pharmacy from Universitat de Barcelona in 2013

Training and Certification

  • GCP Guidelines in 2015 Training
  • Nutrition / Diet Therapy in 2014 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Research Associate (CRA) Clinical Data Manager (DM)
  • Locations I am interested in:
    Germany Spain
  • Work From Home:
    Yes, 0 to 2 days per week
  • International:

Area / Region

Barcelona, Spain


Driving License
  • Yes